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To evaluate and compare the effects of injectable platelet-rich fibrin (i-PRF) which is a third generation platelet concentrate and micro-osteoperforation (MOP) also known as flapless bone puncturing on the rate of canine movement during retraction in patients requiring premolar extractions.

Not Applicable
Conditions
Health Condition 1: K039- Disease of hard tissues of teeth,unspecified
Registration Number
CTRI/2022/12/048404
Lead Sponsor
KUSHAL TAORI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients age varying from 15 â?? 30 years having class 2 division 1 and bimaxillary

protrusion that requires removal of both maxillary first premolars.

2. Patients with average growth pattern.

3. Patients with no systemic conditions and diseases.

4. Patients with fully erupted maxillary canine.

5. Patients with healthy periodontal parameters having no clinical attachment loss or PPD

more than 2-3 mm.

6. Patients indicated for fixed orthodontic therapy.

Exclusion Criteria

1. Patients with horizontal and vertical growth pattern.

2. Patients with developmental and congenital syndromes.

3. Patients with any systemic diseases like clotting disorders and conditions like pregnancy,

anticoagulant therapy.

4. Patients above the age of 30 years.

5. Patients with deleterious habits like smoking are the subjects to be excluded.

6. Patients undergoing removal or myofunctional orthodontic treatment.

7. Patients on medication that decease orthodontic tooth movement like NSAIDS(Ibuprofen,

aspirin, aceclofenac, diclofenac), bisphosphonates, hormonal replacement therapies.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of canine retraction.Timepoint: At T1 T2 T3 T4 <br/ ><br>T1 - one week post extraction <br/ ><br>T2 - four weeks post extraction <br/ ><br>T3 - 8 weeks post extraction <br/ ><br>T4 - 12 weeks post extraction
Secondary Outcome Measures
NameTimeMethod
Pain assessment in both the groups.Timepoint: at T1 T2 T3 T4 where, <br/ ><br>T1 - one week post extraction <br/ ><br>T2 - four weeks post extraction <br/ ><br>T3 - 8 weeks post extraction <br/ ><br>T4 - 12 weeks post extractioon
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